Application of prosthesis eversion method for ascending aorta replacement guarantees better clinical outcomes of type A acute aortic dissection surgery
Introduction
Stanford type A acute aortic dissection (AAD) is one of the most life-threatening disease. Surgery is by far the most effective therapy for type A AAD (1). Meanwhile, it presents severe risk of intra-operative trauma. The main risk factors contributing to it include large intra-operative hemorrhage, profound hypothermia, circulation arrest, and prolonged cardio-pulmonary bypass (CPB) (2).
Being the most complex part of the aorta, the aortic root has a unique configuration with a clover-like dilation of the valsalva sinuses, within which the aortic valve forms a three-pronged crown (3,4). A determining factor for a successful AAD surgery is a reliable proximal anastomosis between the sinusoidal junction and the aortic prosthesis (5). It is advised that the prosthesis is sutured evenly to the autologous aortic wall (5). It is advised that the prosthesis is uniformly sutured to the aortic wall (5). But this is difficult to do practically, especially in the presence of inflammatory edema, as it has a high risk of proximal anastomotic bleeding and high operative mortality.
In 1998, Pretre introduced a new suturing method in ascending aorta replacement (AAR). The most important feature of this method is a prosthesis eversion before and after suturing the prosthesis to the autologous aorta (6). Rignano et al. adopted this method to treat AAD patients (7). But since then, no study has investigated the advantage of this method over the traditional one, especially in AAD surgery. In this study, we aimed to compare the difference of the clinical outcomes between prosthesis eversion and traditional methods by retrospectively analyzing the data from our center. We present the following article in accordance with the STROBE reporting checklist (available at http://dx.doi.org/10.21037/jtd-20-2578).
Methods
Patients
The study was conducted in accordance with the Declaration of Helsinki (as revised in 2013). This study was approved by the Ethics Committee of the Renmin Hospital of Wuhan University, Wuhan, China (NO. 2015-10-19 V1) and informed consent was taken from all the patients.
We retrospectively analyzed the data of a total of 283 patients diagnosed with Stanford type A AAD that were operated in Renmin Hospital of Wuhan University between March, 2006 and April, 2020. Before February, 2020, 88 patients were treated with traditional continuous suture technique. After February 2008, 195 patients were treated with prosthesis eversion method. Patients with genetic disorders like Marfan syndrome or L-D syndrome were excluded from this study. To avoid selection bias, all patients meeting inclusion criteria were included.
Anesthesia and surgical strategies
As we described in a previous study (8), all procedures were performed under general anesthesia and via a standard median sternotomy. CPB with bilateral antegrade cerebral perfusion was used for brain protection. Cannulation of the femoral artery was used for CPB. After CPB was initiated, the temperature gradually lowered. The lowest nasopharyngeal temperatures during circulatory arrest were between 20 to 22 °C.
Apart from this, total or hemi-arch replacement was performed depending on the aortic arch involvement. When the descending aorta was involved, the CRONUS® stented graft was placed in the appropriate segment of the descending thoracic aorta. Coronary artery bypass was performed when coronary artery was involved or coronary artery stenosis was diagnosed.
Platelet (0–6 u) and Coseal surgical sealant (0–4 mL) were used whenever available. Human fibrinogen was used when fibrinogen deficient is diagnosed.
Technical detail of sleeve anastomosis
Proximal ascending aorta anastomosis
Preparation of the vascular prosthesis is illustrated in Figure 1. A suture line was fixed on one end (serves as distal end) in order to turn over the vascular prosthesis (Figure 1A,B). The vascular prosthesis was inserted into the left ventricle until the proximal end of the vascular prosthesis was aligned in parallel with the cut edge of the aortic root (Figure 1C). The aortic prosthesis and the aortic root stump were then sutured in continuous fashion (Figure 2A,B). We think two coils of the prothesis (about 3 mm) are the most suitable for the coaptation between the prothesis and the aortic wall. The fixed line was pulled to take out and turn over the aortic prothesis (Figure 2C,D). A rigid infusion tube was advanced into in the vascular prosthesis, and the entire structure was occluded temporarily with a straight clamp (Figure 2E). Finally, cardioplegic solution was administered through the tube until a pressure around 180±20 mmHg was reached. Anastomosis is strengthened in any area of cardioplegic solution leakage.
Distal ascending aortic anastomosis
About 0.5 cm of the reconstructed ascending aortic prosthesis is folded externally to create a new sutural margin (Figure 3A). Subsequently, the ascending aortic prosthesis can now be connected with the proximal end of the four branched arch prosthesis (Figure 3B). Lastly, ascending aortic prosthesis’ end is then unfolded to compress the anastomosis (Figure 3C).
Clinical information collection and statistical analysis
Baseline data, intra-operative and post-operative data were collected from medical records. Continuous variables were reported as means ± standard deviation or median with ranges and were compared with t-test. Categorical variables were compared using the Chi test and generalized Fisher’s exact test. A P value of <0.05 was considered statistically significant. Analyses were performed with SPSS 19.0.
Results
Baseline data
Baseline data is shown in Table 1. No significant difference of most of the baseline data existed between the two groups, except for age (44.9±16.6 vs. 48.9±12 years), incidence of hyperlipidemia (43/195 vs. 16/88) and taking ACEI/ARB drugs (43/195 vs. 32/88) (P<0.05).
Full table
Intra-operative data
Intra-operative data is provided in Table 2, which showed no difference of surgical methods existed. But cardiopulmonary bypass time, cross-clamp time, circulation arrest time, hemostasis time and total operation time of patients in the traditional anastomosis group were far longer than in patients in the prosthesis eversion group (P<0.01). In addition, the latter received a much smaller amount of RBC and plasma transfusions (P<0.01). The operation mortality is 1/88 and 0/195 in the traditional method and prosthesis eversion group, respectively (P>0.05).
Full table
Early-stage clinical results
Early-stage clinical results are given in Table 3. Ventilation time, post-operative mortality, incidence of re-exploration, tracheostomy, paraplegia, long-term coma and stroke were similar in the two groups (P>0.05). Patients in the traditional method group spent more time in ICU and in hospital than patients in the prosthesis eversion group (P<0.05). Patients in traditional method group accepted more RBC (P<0.01), plasma (P<0.05), human fibrinogen (P<0.01), human albumin (P<0.05) transfusion, and Coseal surgical sealant application (P<0.05) than patients in prosthesis eversion method group.
Full table
Discussion
In this study, we confirmed that prosthesis eversion method is superior to the traditional suturing method characterized by end-to-end anastomosis in AAD treatment. Adequate exposure is crucial to any successful surgery (9). In AAR, the posterior semi-circle of the proximal anastomotic portion has the highest risk of bleeding. When prosthesis eversion method is applied, every part of the anastomotic edge is totally exposed to the surgeons, allowing them to apply sutures to the best of their abilities (10). This advantage was also noted in our experience during using this technique.
Since AAD patients mostly receive emergency surgeries, inflammatory edema is seen surrounding the aortic walls (11). This leads to an increased risk of anastomotic leakage. If bleeding occurs after resuming circulation, adding sutures makes hemorrhage only more severe rather than stopping it. The prothesis eversion method results in eversion, which can improve coaptation area between the prothesis and the aortic wall. It is also much safer to apply extra sutures in case of bleeding.
Our analysis showed prosthesis eversion method can reduce hemostasis time and blood loss, which is of utmost importance for patients undergoing AAR. In spite of homologous transfusion being quite effective treatment of intra-operative blood loss, its side effects can never be completely avoided (12,13). Furthermore, excessive blood loss followed by massive blood transfusion in cardiac surgery is independently associated with serious post-operative complications such as sepsis, acute respiratory distress syndrome, renal failure, and mortality (14-16). Our study also demonstrated that prosthesis eversion method can reduce ventilation time, duration of stay in ICU and in hospital. This may be at least partially attributed to the reduced blood loss and blood products transfusion.
Chronic aortic dissection and aortic aneurysm are not contraindications of the prosthesis eversion method. But hemostasis in case of chronic aortic dissection and aortic aneurysm is much easier than when AAD is diagnosed. Such patients were excluded to make the results of the two groups more comparable.
A major limitation of this study is lies in its retrospective design. So the recommendation yield from our conclusion is low. Prospective controlled studies are required to further verify the effectiveness of and safety of prothesis eversion method.
Conclusions
In conclusion, our experience and statistical analysis showed prosthesis eversion method to have an advantage in reducing blood loss and improving clinical results compared with repair using continuous suture technique. This technique is both simple to learn and perform.
Acknowledgments
Doctor Bulat Abdrakhimov helped us in grammar checking.
Funding: This study was funded by National Natural Science Foundation of China [81570428, 81600367].
Footnote
Reporting Checklist: The authors have completed the STROBE reporting checklist. Available at http://dx.doi.org/10.21037/jtd-20-2578
Data Sharing Statement: Available at http://dx.doi.org/10.21037/jtd-20-2578
Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/jtd-20-2578). The authors have no conflicts of interest to declare.
Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. The study was conducted in accordance with the Declaration of Helsinki (as revised in 2013). This study was approved by the Ethics Committee of the Renmin Hospital of Wuhan University, Wuhan, China (NO. 2015-10-19 V1) and informed consent was taken from all the patients.
Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
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